Cydar , Ltd. is one of 432 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Cydar , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Cydar EV (Series B) and Cydar EV Maps, Cydar EV
2
Total
2
Cleared
0
Denied
Cydar , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Barrington, GB.
Last cleared in 2021. Active since 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cydar , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cydar , Ltd.
2 devices